Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Monday, April 15, 2024

The use of frailty questionnaires in inpatients in two neurorehabilitation units in the East Midlands – A cross-sectional cohort study with follow-up to 1-year after discharge from inpatient rehabilitation

 Is your hospital ready with protocols to get frail stroke survivors to 100% recovery or not? If not, find someplace that is competent in that!

The use of frailty questionnaires in inpatients in two neurorehabilitation units in the East Midlands – A cross-sectional cohort study with follow-up to 1-year after discharge from inpatient rehabilitation

Abstract

Background:

Frailty correlates with poor clinical outcomes and is not routinely assessed in neurorehabilitation inpatient settings.

Methods:

We recruited adults from two neurorehabilitation units. We administered six validated tools for assessing frailty and collected data around length of stay, discharge, readmission and change in rehabilitation outcome measures.

Results:

Seventy-eight participants aged between 31 and 84 years were recruited with a range of neurological diagnoses. Frailty prevalence ranged between 23% and 46%, depending on the scale used, with little agreement between tools. Frailty status did not correlate with age, gender, length of stay, discharge destination and rehabilitation outcome measures. One-year readmission was higher in participants rated as frail by the Frail-Non-Disabled Questionnaire, the FRESH-screening questionnaire and the Clinical Frailty Scale.

Discussion:

Frailty ascertainment was variable depending on the tool used. Three frailty indices predicted readmission rate at 1 year but no other outcome measures. Therefore, frailty tools may have limited utility in this clinical population.

Introduction

Frailty describes loss of physiological reserve and vulnerability to adverse events. It was initially described in older people because it increases in prevalence with age and has explanatory value in understanding how older people respond differentially to acute illness.1 Frailty is associated with adverse outcomes regardless of age.2 The term ‘frailty’ should not be used in populations with life-long impairments but may help understand other patient groups with acquired disabilities who deteriorate physiologically in response to acute insults.
Prognostication in neurorehabilitation is difficult because of multiple complex interacting exposures that determine outcomes.3 Identifying (and addressing) frailty may improve outcomes or help to inform discussions around prognosis and treatment planning.
Two main paradigms describe and measure frailty. The first describes a cascade of homeostatic decompensation and is measured by the presence or absence of physiological parameters (phenotypic frailty).4 The second counts deficits across a number of domains and expresses severity of frailty as a ratio of deficits present to potential deficits (accumulation of deficits).5 Both models select different individuals as being frail but predict adverse outcomes equally well and consensus papers6 have suggested that frailty indices should be selected based upon feasibility and utility in a given clinical context. Most frailty indices have been designed and are primarily used in older populations, and caution should be used when applying them to younger populations.7
Against this background, we set out to evaluate frailty indices in inpatients undergoing neurorehabilitation with the following objectives:
To compare the prevalence of frailty as measured by different frailty measures
To assess differences in frailty between different diagnoses and ages
To assess whether frailty status impacted rehabilitation outcomes
To assess feasibility of assessing frailty using questionnaires during inpatient neurorehabilitation
To assess ease of use of commonly used questionnaires either with patient or next of kin

Methods

This was a two-site study in the East Midlands of England. The sites comprised a 19-bedded level 2b unit and a 25-bedded level 2a unit based within large NHS acute provider trusts.
The study was sponsored by the University of Nottingham and received ethical approval from Yorkshire and The Humber – Leeds East Research Ethics Committee (ref: 18/YH/0361).
Participants were recruited between February 2019 and December 2020, with a hiatus between March and July 2020 (Derby) and March and September 2020 (Nottingham) due to the COVID-19 pandemic.
Patients were eligible for inclusion if they were inpatients in participating units for purposes of neurorehabilitation and aged 18 years or older. They were excluded if they or a consultee were unable or unwilling to give consent.
Potential participants who had capacity to consent to participate in the study gave written informed consent. Participants who lacked capacity and could not give consent were recruited following a discussion with a relevant consultee, such as a family member or friend, in keeping with the provisions of the Mental Capacity Act 2005.8
Baseline constituted the date of admission to the rehabilitation unit. Data collection at baseline comprised participant demographic and clinical details, including diagnosis, comorbidities, age, gender, date of admission to rehabilitation unit and frailty status.
We selected frailty assessment tools which:
Asked about the period of time before the hospital admission as being representative of a patient’s baseline function
Did not require invasive testing for example, blood tests/muscle biopsies
Did not rely on tests which could have been altered by recent inpatient stay or intercurrent illness (e.g. serum albumin)
Could be answered by next of kin/consultee if the participant was cognitively impaired and unable
Could be carried out quickly and simply on an inpatient unit, with minimal disruption to daily care
Had been used and validated in clinical settings
Required no special training to perform
On this basis we recorded:
The Clinical Frailty Scale (CFS) – uses a nine-item scale to categorise individuals on the spectrum of ‘very fit’ to ‘terminally ill’9
Fatigue/Resistance/Ambulation/Illness/Loss of weight scale (FRAIL) – a five-item questionnaire (covers fatigue/resistance/ambulation/illnesses/loss of weight); individuals are divided into ‘frail’, ‘pre-frail’ or ‘robust’ depending on their score10
Frail non-disabled questionnaire (FIND) – a brief, five item questionnaire which asks about walking, climbing stairs, weight loss, fatigue and physical activity; it categorises respondents into ‘robust/disabled/frail/frail and disabled’11
FRESH-screening instrument – a four-question tool (around mobility/fatigue/falls/assistance); individuals are characterised as ‘normal’ or ‘frail’12
Groningen Frailty Index (GFI) – a 15-question questionnaire that covers the domains of mobility, vision, hearing, nutrition, comorbidity, cognition, psychosocial and physical fitness, with the total score dividing respondents into ‘frail’ or ‘non-frail’13
Modified Reported Edmonton Frail Scale (m-REFS) – removes the question which asks the patient to draw a clock and instead replaces it with a question around a history of cognitive impairment, shown to be equivalent to the Reported Edmonton Frail Scale in a prospective cohort study.14 The original Edmonton frail scale is valid and reliable15; this had been modified slightly to allow it to be answered by next of kin and trialled successfully. Respondents are classified as ‘not frail’/‘apparently vulnerable’/ ‘mildly frail’/‘moderately frail’/‘severely frail’.14
For the sake of simplicity, the scores were divided into ‘frail’ and ‘non-frail’/‘robust’ as shown in Table 1:

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